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Clinical Study on the Efficacy of Traditional Chinese Medicine in the Treatment of Lymphatic Leakage after Pelvic Lymphadenectomy

Clinical Study on the Efficacy of Traditional Chinese Medicine in the Treatment of Lymphatic Leakage after Pelvic Lymphadenectomy

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081955
Enrollment
Unknown
Registered
2024-03-18
Start date
2024-03-18
Completion date
Unknown
Last updated
2024-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder Cancer

Interventions

intervention group:Jindan With Extension Granules, Specification: 15g/bag, provided by Jiangxi Huatai Pharmaceutical Co. Usage: administered after exhaustion, boiled water for 12 days. Routine dosage:
Control group:None

Sponsors

Second Hospital of Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Men or women aged 18 years and above; 2. patients after radical total cystectomy with lymphatic clearance 3. expected survival time is large 4. subjects voluntarily enrolled in the study, signed the informed consent, complied well and cooperate with follow-up visits.

Exclusion criteria

Exclusion criteria: 1. Hypersensitivity to the components of the drugs used in this test; 2.Combined with liver, kidney (alanine aminotransferase, glutamic oxal transaminase =1.5 times the upper limit of normal value, blood creatinine exceeds the upper limit of normal value) and hematopoietic system and other serious primary (alanine transaminase, glutamic transaminase =1.5 times the upper limit of normal value, blood creatinine exceeds the upper limit of normal value) and hematopoietic system and other serious primary Patients with severe primary diseases such as liver, kidney (alanine aminotransferase =5 times the upper limit of normal value, blood creatinine exceeding the upper limit of normal value, hematopoietic system, etc.) and psychiatric diseases; 3. Those who have been examined and confirmed to have symptoms caused by other diseases; 4. Patients who have undergone other treatments related to the disease within two weeks; 5. Patients with severe coagulation disorders; 6. patients who are participating in other clinical trials; 7. patients with suspected or confirmed history of alcohol or drug abuse; 8.Those who, in the opinion of the investigator, are unsuitable for enrollment in this trial for other reasons.

Design outcomes

Primary

MeasureTime frame
volume of drainage;

Secondary

MeasureTime frame
Quality of life score;

Countries

China

Contacts

Public ContactHu Hailong

Second Hospital of Tianjin Medical Univertsity

13100950133@163.com+86 136 6209 6232

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026